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94225-32-8

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94225-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94225-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94225-32:
(7*9)+(6*4)+(5*2)+(4*2)+(3*5)+(2*3)+(1*2)=128
128 % 10 = 8
So 94225-32-8 is a valid CAS Registry Number.

94225-32-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name c-2-chloro-1-phenacylcyclohexan-r-1-ol

1.2 Other means of identification

Product number -
Other names 2-((1S,2S)-2-Chloro-1-hydroxy-cyclohexyl)-1-phenyl-ethanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:94225-32-8 SDS

94225-32-8Downstream Products

94225-32-8Relevant articles and documents

Catalytic Effect of Five-Coordinate Organotin Bromide or Tetraphenylstibonium Bromide on the Chemo- and Stereoselective Addition of Tin Enolate to α-Halo Ketone

Yasuda, Makoto,Oh-hata, Tatsuhiro,Shibata, Ikuya,Baba, Akio,Matsuda, Haruo,Sonoda, Noboru

, p. 1180 - 1186 (1995)

Two types of catalysts, five-coordinate organotin bromides and tetraphenylstibonium bromide, similarly promoted the selective addition of tin enolates to the carbonyl moiety in α-halo ketones.The reaction with 2-chlorocyclohexanones and the enolates gave

REACTION OF α-CHLOROKETONES WITH 1,4-DIANION OF ACETOPHENONE N-ETHOXYCARBONYLHYDRAZONE

Matsumura, Noburu,Kunugihara, Akira,Yoneda, Shigeo

, p. 4529 - 4532 (2007/10/02)

1,4-Dianion of acetophenone N-ethoxycarbonylhydrazone (2) reacts with α-chloroketones such as phenacyl chloride, 1-chloroacetone, 3-chloro-2-butanone, and 1,3-dichloroacetone to give pyrazoline derivatives in good yields.In the reactions of 2-chlorocyclohexanone and 3-chloro-2-norbornanone with 2, cis-chlorohydrin and exo-chlorohydrin were selectively obtained, respectively.

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